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Axsome Therapeutics to Report Second Quarter 2024 Financial Results on August 5

Axsome Therapeutics to Report Second Quarter 2024 Financial Results on August 5

axsome therapeutics將於2024年8月5日公佈第二季度業績。
Axsome Therapeutics ·  07/11 00:00
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NEW YORK, July 11, 2024 (GLOBE NEWSWIRE) -- Axsome Therapeutics, Inc. (NASDAQ: AXSM), a biopharmaceutical company developing and delivering novel therapies for the management of central nervous system (CNS) disorders, today announced it will report its financial results for the second quarter of 2024 on Monday, August 5, 2024, before the opening of the U.S. financial markets. Axsome's management team will host a conference call at 8:00 a.m. Eastern Time on August 5, 2024, to discuss these results and provide a business update.

納斯達克(NASDAQ)上市的生物製藥公司Axsome Therapeutics, Inc. (AXSM)致力於開發和提供用於管理中樞神經系統(CNS)疾病的新型療法,於2024年8月5日美國金融市場開盤前公佈2024年第二季度業績。Axsome的管理團隊將於2024年8月5日上午8:00(美國東部時間)舉行電話會議,討論這些結果並提供業務更新。

To participate in the live conference call, please dial (877) 405-1239 (toll-free domestic). A live webcast of the conference call can be accessed on the "Webcasts & Presentations" page of the "Investors" section of the Company's website at . A recording of the conference call will be available on the Company's website for approximately 30 days following the live event.

請撥打電話(877)405-1239(國內免費),參加現場電話會議。可以通過公司網站上“Webcasts&Presentations”頁面訪問電話會議的現場網絡廣播。電話會議的記錄將在現場活動後大約30天內在公司網站上提供訪問。

About Axsome Therapeutics, Inc.

關於Axsome Therapeutics公司,Inc。

Axsome Therapeutics, Inc. is a biopharmaceutical company developing and delivering novel therapies for central nervous system (CNS) conditions that have limited treatment options. Through development of therapeutic options with novel mechanisms of action, we are transforming the approach to treating CNS conditions. At Axsome, we are committed to developing products that meaningfully improve the lives of patients and provide new therapeutic options for physicians. For more information, please visit the Company's website at axsome.com. The Company may occasionally disseminate material, nonpublic information on the company website.

Axsome Therapeutics,Inc.是一家生物製藥公司,開發和提供中樞神經系統(CNS)條件創新療法,治療選擇有限的情況。通過開發具有新的作用機制的治療選擇,我們正在改變治療中樞神經系統疾病的方法。在Axsome,我們致力於開發能夠顯著改善患者生命和爲醫生提供新的治療選擇的產品。有關更多信息,請訪問公司網站axsome.com。該公司可能偶爾在公司網站上發佈非公開信息。

Forward Looking Statements

前瞻性聲明

Certain matters discussed in this press release are "forward-looking statements". We may, in some cases, use terms such as "predicts," "believes," "potential," "continue," "estimates," "anticipates," "expects," "plans," "intends," "may," "could," "might," "will," "should" or other words that convey uncertainty of future events or outcomes to identify these forward-looking statements. In particular, the Company's statements regarding trends and potential future results are examples of such forward-looking statements. The forward-looking statements include risks and uncertainties, including, but not limited to, the continued commercial success of our Sunosi and Auvelity products and the success of our efforts to obtain any additional indication(s) with respect to solriamfetol and/or AXS-05; the success, timing and cost of our ongoing clinical trials and anticipated clinical trials for our current product candidates, including statements regarding the timing of initiation, pace of enrollment and completion of the trials (including our ability to fully fund our disclosed clinical trials, which assumes no material changes to our currently projected revenues or expenses), futility analyses and receipt of interim results, which are not necessarily indicative of the final results of our ongoing clinical trials, and/or data readouts, and the number or type of studies or nature of results necessary to support the filing of a new drug application ("NDA") for any of our current product candidates; our ability to fund additional clinical trials to continue the advancement of our product candidates; the timing of and our ability to obtain and maintain U.S. Food and Drug Administration ("FDA") or other regulatory authority approval of, or other action with respect to, our product candidates, including statements regarding the timing of any NDA submission; whether issues identified by FDA in the complete response letter may impact the potential approvability of the Company's NDA for AXS-07 for the acute treatment of migraine in adults with or without aura, pursuant to our special protocol assessment for the MOMENTUM clinical trial; the Company's ability to successfully defend its intellectual property or obtain the necessary licenses at a cost acceptable to the Company, if at all; the successful implementation of the Company's research and development programs and collaborations; the success of the Company's license agreements; the acceptance by the market of the Company's products and product candidates, if approved; the Company's anticipated capital requirements, including the amount of capital required for the continued commercialization of Sunosi and Auvelity and for the Company's commercial launch of its other product candidates, if approved, and the potential impact on the Company's anticipated cash runway; unforeseen circumstances or other disruptions to normal business operations arising from or related to geo-political conflicts or a global pandemic and other factors, including general economic conditions and regulatory developments, not within the Company's control. The factors discussed herein could cause actual results and developments to be materially different from those expressed in or implied by such statements. The forward-looking statements are made only as of the date of this press release and the Company undertakes no obligation to publicly update such forward-looking statements to reflect subsequent events or circumstance.

本新聞稿中討論的某些事項是“前瞻性聲明”。我們在某些情況下使用“預測”,“相信”,“潛力”,“繼續”,“估計”,“預期”,“計劃”,“打算”, “可能”,“可能”,“將”,“應該”或其他傳達未來事件或結果的不確定性的單詞來識別這些前瞻性聲明。特別是,公司關於趨勢和潛在未來結果的陳述是此類前瞻性聲明的示例。前瞻性聲明包括風險和不確定性,包括但不限於繼續商業化Sunosi和Auvelity產品的成功以及我們取得任何關於solriamfetol和/或AXS-05的額外指示(s)的努力成功;我們當前product候選者的進行中的臨床試驗以及預期的臨床試驗的成功,包括有關試驗啓動的時間,招募步伐和完成情況的陳述(包括我們能否全額資助所披露的臨床試驗,這假設我們當前預計的收入或支出未發生實質性變化),無效分析和獲得中期結果,不一定是正在進行的臨床試驗的最終結果,和/或數據讀取,及支持提出新藥申請(“NDA”)所需的研究數量或類型或結果的性質(目前的任何product候選者);我們能夠爲繼續推進我們的product候選者而資助額外的臨床試驗的時間;我們獲得並維護美國食品和藥物管理局(“FDA”)或其他監管機構批准或採取行動的時間與能力涉及我們的product候選者,包括有關提交任何NDA的時間的聲明;是否FDA在完整回覆信中確定的問題可能會影響AXS-07 NDA的潛在批准性,用於有或無視幻象的成人偏頭痛,依據我們對MOMENTUm臨床試驗的特殊協議評估;本公司成功捍衛其知識產權或以可接受成本獲得必要的許可證,如果有的話;本公司的研究和開發計劃和合作的成功實施;本公司授權協議的成功;市場對公司產品和product候選者(如果獲得批准)的接受程度;我們所預計的資本需求,包括繼續商業化Sunosi和Auvelity的資本要求以及本公司商業化其他product候選者的資本要求(如果獲得批准),以及本公司預期現金離岸期潛在影響;由地緣政治衝突或全球大流行引起的或與之相關的其他未預料到的情況或其他干擾正常業務運營的因素,包括但不限於總體經濟條件和監管發展,不在公司控制範圍內。所討論的因素可能會導致實際結果和發展與所述聲明中明示或暗示的結果和發展有實質不同。前瞻性聲明僅作爲本新聞稿的發佈日期,並且本公司無義務公開更新此類前瞻性聲明以反映隨後發生的事件或情況。

Axsome Contacts:

Axsome聯絡人:

Investors:
Mark Jacobson
Chief Operating Officer
Axsome Therapeutics, Inc.
One World Trade Center, 22nd Floor
New York, NY 10007
Tel: 212-332-3243
Email: mjacobson@axsome.com

投資者:
馬克·雅各布森
首席運營官
Axsome Therapeutics公司
One World Trade Center,22樓
紐約市10007
電話:212-332-3243
電子郵件:mjacobson@axsome.com

Media:
Darren Opland
Director, Corporate Communications
Axsome Therapeutics, Inc.
One World Trade Center, 22nd Floor
New York, NY 10007
Tel: 929-837-1065
Email: dopland@axsome.com

媒體:
Darren Opland
董事,企業通信
Axsome Therapeutics公司
One World Trade Center,22樓
紐約市10007
電話:929-837-1065
電子郵件:dopland@axsome.com


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Source: Axsome Therapeutics, Inc.

來源:Axsome Therapeutics,Inc。

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